ENST00000682153.1:c.*1573C>T
(VPS13B)
|
ENSP00000507923.1:n.*1573C>T
|
|
ENST00000682358.1:n.12549C>T
(VPS13B)
|
|
|
ENST00000683334.1:c.*7601C>T
(VPS13B)
|
ENSP00000507369.1:n.*7601C>T
|
|
ENST00000357162.7:c.11844C>T
(VPS13B)
MANE Select
|
ENSP00000349685.2:p.Ser3948=
|
|
ENST00000358544.7:c.11919C>T
(VPS13B)
MANE Plus Clinical
|
ENSP00000351346.2:p.Ser3973=
|
|
ENST00000357162.6:c.11844C>T
(VPS13B)
|
ENSP00000349685.2:p.Ser3948=
|
|
ENST00000358544.6:c.11919C>T
(VPS13B)
|
ENSP00000351346.2:p.Ser3973=
|
|
ENST00000493587.1:n.1421C>T
(VPS13B)
|
|
|
ENST00000520517.5:c.*142-424G>A
(COX6C)
|
ENSP00000429991.1:n.*142-424G>A
|
|
ENST00000522934.5:c.*142-2223G>A
(COX6C)
|
ENSP00000428702.1:n.*142-2223G>A
|
|
NM_017890.4:c.11919C>T , LRG_351t1:c.11919C>T
(VPS13B)
|
NP_060360.3:p.Ser3973=
|
|
NM_152564.4:c.11844C>T , LRG_351t2:c.11844C>T
(VPS13B)
|
NP_689777.3:p.Ser3948=
|
|
XM_005250800.2:c.11919C>T
(VPS13B)
|
XP_005250857.1:p.Ser3973=
|
|
XM_005250801.3:c.11919C>T
(VPS13B)
|
XP_005250858.1:p.Ser3973=
|
|
XM_011516848.1:c.11916C>T
(VPS13B)
|
XP_011515150.1:p.Ser3972=
|
|
XM_011516849.1:c.11841C>T
(VPS13B)
|
XP_011515151.1:p.Ser3947=
|
|
XM_011516850.1:c.11541C>T
(VPS13B)
|
XP_011515152.1:p.Ser3847=
|
|
XM_011516851.1:c.8805C>T
(VPS13B)
|
XP_011515153.1:p.Ser2935=
|
|
XM_011516852.1:c.8805C>T
(VPS13B)
|
XP_011515154.1:p.Ser2935=
|
|
XM_011516854.1:c.7698C>T
(VPS13B)
|
XP_011515156.1:p.Ser2566=
|
|
XM_005250800.3:c.11919C>T
(VPS13B)
|
XP_005250857.1:p.Ser3973=
|
|
XM_005250801.5:c.11919C>T
(VPS13B)
|
XP_005250858.1:p.Ser3973=
|
|
XM_011516848.2:c.11916C>T
(VPS13B)
|
XP_011515150.1:p.Ser3972=
|
|
XM_011516849.2:c.11841C>T
(VPS13B)
|
XP_011515151.1:p.Ser3947=
|
|
XM_011516850.2:c.11541C>T
(VPS13B)
|
XP_011515152.1:p.Ser3847=
|
|
XM_011516851.2:c.8805C>T
(VPS13B)
|
XP_011515153.1:p.Ser2935=
|
|
XM_011516852.2:c.8805C>T
(VPS13B)
|
XP_011515154.1:p.Ser2935=
|
|
XM_011516854.2:c.7698C>T
(VPS13B)
|
XP_011515156.1:p.Ser2566=
|
|
XM_017013109.1:c.11724C>T
(VPS13B)
|
XP_016868598.1:p.Ser3908=
|
|
XM_017013111.1:c.8805C>T
(VPS13B)
|
XP_016868600.1:p.Ser2935=
|
|
XM_017013112.1:c.7476C>T
(VPS13B)
|
XP_016868601.1:p.Ser2492=
|
|
XM_024447074.1:c.10704C>T
(VPS13B)
|
XP_024302842.1:p.Ser3568=
|
|
NM_017890.5:c.11919C>T
(VPS13B)
MANE Plus Clinical
|
NP_060360.3:p.Ser3973=
|
|
NM_152564.5:c.11844C>T
(VPS13B)
MANE Select
|
NP_689777.3:p.Ser3948=
|
|